Regulation of vertebrate nervous system alternative splicing and development by an SR-related protein
Open accessAbstract
Alternative splicing is a key process underlying the evolution of increased proteomic and functional complexity and is especially prevalent in the mammalian nervous system. However, the factors and mechanisms governing nervous system-specific alternative splicing are not well understood. Through a genome-wide computational and expression profiling strategy, we have identified a tissue- and vertebrate-restricted Ser/Arg (SR) repeat splicing factor, the neural-specific SR-related protein of 100 kDa (nSR100). We show that nSR100 regulates an extensive network of brain-specific alternative exons enriched in genes that function in neural cell differentiation. nSR100 acts by increasing the levels of the neural/brain-enriched polypyrimidine tract binding protein and by interacting with its target transcripts. Disruption of nSR100 prevents neural cell differentiation in cell culture and in the developing zebrafish. Our results thus reveal a critical neural-specific alternative splicing regulator, the evolution of which has contributed to increased complexity in the vertebrate nervous system.
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nSR100 has the strongest neuronal-specific expression relative to the other splicing regulators.
“Moreover, an analysis of RNA-Seq data from different neural cell types (Zhang et al., 2014) revealed that nSR100 has the strongest neuronal-specific expression relative to the other splicing regulators (Figure S4I, and data not shown), which is also consistent with its immunohistochemical detection in neurons but not glia (Calarco et al., 2009).”
From A Highly Conserved Program of Neuronal Microexons Is Misregulated in Autistic Brains (2014) · cites this paper as Calarco et al., 2009
nSR100 promotes neurite outgrowth.
“we have previously shown that nSR100 promotes neurite outgrowth (Calarco et al., 2009)”
From A Highly Conserved Program of Neuronal Microexons Is Misregulated in Autistic Brains (2014) · cites this paper as Calarco et al., 2009
SRRM4 is unique for its brain-specific expression.
“but is unique for its brain-specific expression29.”
From The neurogenetics of alternative splicing (2016) · cites this paper as [29]
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References 36 · Cited by 225
- Authors
- Calarco, J. A., Superina, S., O'Hanlon, D., Gabut, M., Raj, B., Pan, Q., Skalska, U., Clarke, L., Gelinas, D., van der Kooy, D., Zhen, M., Ciruna, B., & Blencowe, B. J.
- Affiliations
- University of Toronto (CA)
- Mount Sinai Hospital (CA)
- King's College London (GB)
- Corresponding author
- Blencowe, Benjamin J.
- Venue
- Cell
- Publisher
- Elsevier BV
- Published
- 2009-09
- Volume
- 138
- Issue
- 5
- Pages
- 898-910
- ISSN
- 0092-8674 (ISSN-L)
- OpenAlex
- W2029824528
- Cited by
- 225
- References
- 36
- Citations by year
- 2026: 5 · 2025: 12 · 2024: 13 · 2023: 13 · 2022: 14 · 2021: 12 · 2020: 10 · 2019: 14 · 2018: 19 · 2017: 14 · 2016: 11 · 2015: 11 · 2014: 14 · 2013: 12 · 2012: 18
- FWCI
- 6.84
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- www.elsevier.com/tdm/userlicense/1.0/ (tdm)
- www.elsevier.com/legal/tdmrep-license (tdm)
- www.elsevier.com/open-access/userlicense/1.0/ (vor, 1415 d)
- doi.org/10.15223/policy-017 (stm-asf)
- doi.org/10.15223/policy-037 (stm-asf)
- doi.org/10.15223/policy-012 (stm-asf)
- doi.org/10.15223/policy-029 (stm-asf)
- doi.org/10.15223/policy-004 (stm-asf)
- Locations
- Cell (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA Research and Splicing
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA regulation and disease
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
- Keywords
- alternative splicing, SR proteins, splicing factors, neural cell differentiation, polypyrimidine tract-binding protein, RNA-binding proteins
- MeSH terms
- Serine-Arginine Splicing Factors, Animals, Brain, Cell Differentiation, Cell Line, Humans, Nerve Tissue Proteins, Neurons, Nuclear Proteins, RNA-Binding Proteins, Alternative Splicing, Mice
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